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Tetramethylthiourea

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Tetramethylthiourea Basic information

Product Name:
Tetramethylthiourea
Synonyms:
  • TETRAMETHYLTHIOUREA
  • 1,1,3,3-TETRAMETHYL-2-THIOUREA
  • 1,1,3,3-TETRAMETHYLTHIOUREA
  • ((CH3)2N)2CS
  • 1,1,3,3-tetramethyl-2-thio-ure
  • Basthioryl
  • N,N,N',N'-Tetramethylthiourea
  • Tetramethylthiourea Synonyms N,N,N',N'-Tetramethylthiourea
CAS:
2782-91-4
MF:
C5H12N2S
MW:
132.23
EINECS:
220-488-0
Product Categories:
  • Heterocycles
  • Organic Building Blocks
  • Sulfur Compounds
  • Thioureas
  • 2782-91-4
Mol File:
2782-91-4.mol
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Tetramethylthiourea Chemical Properties

Melting point:
75-77 °C (lit.)
Boiling point:
245 °C (lit.)
Density 
1.005 (estimate)
refractive index 
1.5300 (estimate)
Flash point:
190 °C
storage temp. 
2-8°C
solubility 
32g/l
form 
solid
pka
1.50±0.50(Predicted)
color 
Off-White to Pale Beige
Water Solubility 
32 g/L (20 ºC)
BRN 
1744916
InChIKey
MNOILHPDHOHILI-UHFFFAOYSA-N
CAS DataBase Reference
2782-91-4(CAS DataBase Reference)
NIST Chemistry Reference
Thiourea, tetramethyl-(2782-91-4)
EPA Substance Registry System
Tetramethylthiourea (2782-91-4)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-20/21/22
Safety Statements 
22-24/25-36
WGK Germany 
3
RTECS 
YU2750000
TSCA 
Yes
HS Code 
29309070
Hazardous Substances Data
2782-91-4(Hazardous Substances Data)

MSDS

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Tetramethylthiourea Usage And Synthesis

Chemical Properties

COLORLESS TO YELLOW CRYSTALLINE CHUNKS

Uses

As a drug.

Uses

Tetramethylthiourea forms BF3 adduct with tetramethylselenourea.

Definition

ChEBI: Tetramethylthiourea is a member of thioureas.

General Description

White crystals.

Air & Water Reactions

Water soluble.

Reactivity Profile

An organosulfide amide. Organosulfides are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).

Hazard

Moderately toxic by ingestion.

Fire Hazard

Flash point data for Tetramethylthiourea are not available, but Tetramethylthiourea is probably combustible.

Safety Profile

Moderately toxic by ingestion. Questionable carcinogen with experimental carcinogenic and teratogenic data. Human mutation data reported. When heated to decomposition it emits very toxic fumes of NOx and SOx. See also SULFIDES.

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